US2492443A - Process for the production op - Google Patents

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US2492443A
US2492443A US2492443DA US2492443A US 2492443 A US2492443 A US 2492443A US 2492443D A US2492443D A US 2492443DA US 2492443 A US2492443 A US 2492443A
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B3/00—Preparation of cellulose esters of organic acids
    • C08B3/16—Preparation of mixed organic cellulose esters, e.g. cellulose aceto-formate or cellulose aceto-propionate

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  • Cellulose fibers have an extremely high degree of plasticity which is accompanied by low elasticity, and tend to undergo irreversible flow under moderate stresses. Products molded from cellulose or its derivatives, such as cellulose esters, exhibit the same properties and tend to become dethis tendency is not reversed and the products do not revert to their original form when the stress is removed.
  • the esters preferably contain from about one or less than one radical derived from the agent capable of reacting bifunctionally with cellulose per about anhydro glucose units to one or less than one such radical per 500 anhydro glucose units or more.
  • the ratio of the modifying radicals to glucose units may vary, but
  • the resulting product is extremely rigid and nonplastic.
  • the radicals derived from agents capable of reacting bifunctionally with cellulose may be introduced simultaneously with or, in some cases, prior to the production of the esters.
  • At least one monobasic organic acid radical and at least one polybasic organic acid radical are introduced simultaneously into cellulose by reaction thereof with a monofunctional esterifying reagent and an esterifying agent capable of re- "acting bifunctionally with cellulose, the reaction being carried out in the presence of a substance in which the reaction product is at least partially solvated, that is, dissolved or swollen as it is formed during the reaction.
  • Suitable monofunctional reagents are monobasic organic acids, such as acetic, propionic,
  • Suitable bifunctionally reacting agents are such polybasic organic acids as adipic, succinic, sebacic acids, etc., as well as polyhalides of such acids.
  • Such diacids derived from glycol may be prepared by the general procedure described by Bruson, Journal American Chemical Society 64, pages 2457 and 2850.
  • cellulose is simultaneously reacted with at least one polybasic organic acid, and at least one anhydride of a monobasic organic acid capable of esterifying cellulose, in the presence of a catalyst, which may be a mineral acid catalyst, for example, and a substance in which the reaction product is dissolved or swollen. during the reaction.
  • a catalyst which may be a mineral acid catalyst, for example, and a substance in which the reaction product is dissolved or swollen. during the reaction.
  • the cellulose may be simultaneously reacted With at least one monobasic organic acid, and at least one polybasic organic acid, in the presence of an impeller which may be an anhydride of a halogen-substituted monobasic organic acid, a catalyst, and a substance in which the reaction product is dissolved or swollen during the reaction.
  • Acid halides may also be used.
  • the cellulose may be reacted simultaneously with at least one monobasic organic .acid halide, and at least one polybasic organic acid halide, in the presence of a condensing agent which is inert with respect to the halides, such as an organic base as for instance, the tertiary amines, pyridine, quinoline, n-methyl morpholine, etc., in the presence of a solvent or swelling agent for the reaction product.
  • a condensing agent which is inert with respect to the halides
  • an organic base as for instance, the tertiary amines, pyridine, quinoline, n-methyl morpholine, etc.
  • introduction of the polybasic organic acid radicals may be effected, in some cases, prior to esterification of the cellulose with a monobasic organic acid.
  • cellulose may be reacted with one or more diacids derivedfromglycol, or dihalides of suchacids, in the presence of a condensing agent or catalyst, and the product thus obtained may then be subsequently reacted with at least one monobasic organic acid, in the usual manner.
  • reaction is carried out in the presence of a substance in which the reaction product is dissolved or swollen as it is formed during the course of the reaction, which results inthe reaction mass being maintained ina highly swollen or dissolved state and thus insures substantially uniform reaction between the cellulose and the monofunctional and bifunctional reagents.
  • a substance in which the reaction product is dissolved or swollen as it is formed during the course of the reaction which results inthe reaction mass being maintained ina highly swollen or dissolved state and thus insures substantially uniform reaction between the cellulose and the monofunctional and bifunctional reagents.
  • substances are, for example, toluene, dioxane, acetone, etc.
  • the final products which may be obtained by precipitating thereaction. mass from. water, may be soluble or substantially insoluble in such substances.
  • the amount of monofunctional reagent used may vary, but in general I prefer'to use an amount thereof sufiicient to form a tri-ester;
  • the tri-ester may be suitably hydrolyzed by conventional methods, after'completion of. the reaction with the bifunctionally reacting esterification agent.
  • bifunctional esterification agent By the choice of bifunctional esterification agent; and the amount thereof participatin in thereaction, it is possible to selectively adjust certain physical properties of the final products, such as solubilities and softening temperatures. Althoughin-all cases the-modified esters show a lesser degree of plasticity and a greater degree of elasticity, and. in general much. higher softening and melting temperatures and resistance to common solvents, as compared with corresponding cellulose esters which do not contain the modifying-groups, modified esters may also be obtained which do not greatly differ from the unmodified l esters in respect of solubility and softening temperatures.
  • the degree to which the final modified esters are soluble in substances which are solvents for cellulose esters, such as acetone, dioxane, toluene; etc., for instance, may vary, depending upon the amount of bifunctional esterification agent used, greater amounts decreasing the solubility and lesser amounts increasing it.
  • the modified esters do not have melting points below decomposition temperatures or sharp softening points, are substantially unafiected at temperatures at which the unmodified esters melt or' soften, do not show a tendency to soften except within high temperature ranges, and at temperaturesabove the softening range are less plasticand more rubberlike than unmodified esters.
  • the softening temperature in some instances may be varied, dependin upon. the amount and.
  • bifunctional esterification agent used,.the tendency to soften at relatively low temperatures being more marked in those cases. wheresuch agent is used in relatively smallamounts and has a longer chain as compared to the ester side chain derived from the. monobasic acid.
  • the use of marginal amounts of the bifunctional esterification agent in. the reaction thus permits a sensitive adjustment of the solubility and soft ening characteristics of the end, product.
  • the amount of such agent to be used depends upon the properties desired in the final products.
  • the bifuncti'onally reacting agent such as the dihalide of an organic dibasic acid
  • the bifuncti'onally reacting agent such as the dihalide of an organic dibasic acid
  • the final product containing, usually, one or less than one dibasic acid radical. per 20 anhydro glucose units, to one or less than one dibasic acid radical per 500 anhydro glucose units, or more.
  • the products are obtained in the form of fibrous masses which are, for the most part, insoluble, infusible, and heat-insensitive, but which in certain cases, as previously indicated, may be soluble to varying extents and more or less susceptible to softening by heat.
  • Some of the insoluble or substantially insoluble modified esters, such as cellulose butyrate containin sebacic acid radicals may be molded by compression and injection molding techniques to give molded articles which are characterized by hardness, resistance to cold flow, and resistance to flow at elevated. temperatures.
  • the molded products may undergosome flow under stress but due to their quality of rapid and-substantially complete elastic recovery, show a. lively return to their original form. upon the removal of. stress.
  • Those products which. are soluble. in-. solvents such as acetone, for example, may be dissolved therein and extruded through a-spinneret or the like into an evaporative atmosphere, in accordance with the dry-spinning process,.to form artificial filaments, or may be cast from such solutions to give films, sheets, coatings etc.. which are durable and stable.
  • substances may be added to the products to give various effects. Some of. the
  • coloring materials such as dyes, pigments, particles of colored materials to give-mottled effects, metallic particlesorthe like.
  • the products exhibit properties suchas alesser degree of plasticity, greatly increased. elasticity, generally increased softening. and melting. temperature ranges, and rang of. solubilit incommon solvents which are. distinctly diflierent. from the properties of corresponding, cellulose. esters, such as cellulose laurate, cellulose propionate, etc., which do not containthe. chemically cornbined modifying polybasic acid radicals. While the reasons for the marked changein properties cannot be stated precisely, itisbelieved that the change may be predicated. upon. a chemica1.reaction of the polybasicacidsortheir halides-with hydroxyl groups on parallel. cellulosechains, so that cross-links are formedbetween the primary valence chains of. the. cellulose derivatives.
  • the introduction'of the radical or radicals. derivedfrom thebifunctional esterification agent may be effected simultaneously with, or in some instances, prior to substantial esterification of the. cellulose. with the monobasic acids or their. halides, when the reaction is carried out.in.the presence ofasolveht capable of swelling, or dissolving the reaction product as: it is formed. during the reaction.
  • Example II The reaction was carried out in accordance with the procedure described in Example 1, except that a 5% solution of 0.1 part of sebacoyl chloride were added to 40 parts of lauroyl chloride, and that mixture was added dropwise to the Wood pulp suspension. After precipitating product (yield: 87% based on as a fibrous white mass which was insoluble in toluene, did not soften below 210 0., and had no melting point.
  • Example III Eight parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and 100 parts of dioxane, and the suspension was heated to 60 to 80 C. A 5% solution of 0.06 part of sebacoyl chloride in toluene was added to 32 parts of butyryl chloride, and that mixture was added dropwise, with constant stirring, to the suspension. The mixture was heated to IS-85 C. for 2 hours. The reaction product (yield: 83% based on tri-butyrate) was precipitated and leached with water and a fibrous white mass was obtained, which was insoluble in acetone, and had a softening range of 130-135 C. The softening range of unmodified ⁇ cellulose butyrate prepared under similar conditions was found to be 125-l30 C.
  • Example IV The procedure was the same as described in Example III except that a 5% solution of 0.01 part of sebacoyl chloride was added to 32 parts of butyryl chloride, and that mixture was added drop-Wise to the wood pulp suspension. The final product (yield: about 91% based on tributyrate) was precipitated and leached with water. A fibrous white mass was obtained which was soluble in acetone, had a softening range of 130-135 C., and could be drawn into filaments at 180-200" C.
  • Example V Five parts air-dry wood pulp were suspended in a mixture of 50 parts of pyridine and 80 parts of dioxane and the suspension was heated to 60-85" C. A mixture of 26 parts of caproyl chloride and 0.08 part of succinyl chloride was addpionate) was a fibrous white mass ed dropwise to the above suspension, and the whole was heated at '75-85 C. for about 3 hours. After precipitating and leaching with water, the product was obtained as a white fibrous mass (yield: about 6% based on tricaproate). The product formed a very stiff gel in dioxane, and had a softening range of 120-l30 C. Unmodifled cellulose caproate prepared under similar conditions softened at about C.
  • Example VI Five parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and parts of dioxane, and the suspension was heated to 60-80 C. 0.2 part of hexaglycol diacid chloride was mixed with 28 parts of propionyl chloride, and added dropwise to the wood pulp suspension: the mixture was kept at 75-85" C. for 3 hours. After precipitating. and leaching with water the final product (yield:-97% based on tri-propionate) occurred in the form of a white mass which was soluble in acetone, had a softening range of -l60 C., and could be drawn to coarse filaments at about 200 C.
  • Example VII Five parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and 100 parts of dioxane, and the suspension was heated to 60-80 C. A mixture of 0.6 part of triglycol diacid chloride and 28 parts of propionyl chloride was added dropwise to the suspension, and the whole was heated at 75-85 C. for 2% hours. After precipitating and leaching the reaction product with water, a fibrous white mass was obtained (yield: 99% based on tri-propionate). The product formed a. grainy solution in acetone, and had softenin range of l55-160 C. Unmodified cellulose propionate softened at about 155 C.
  • Example VIII Five parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and 100 parts of dioxane, and the suspension was heated to 60-80 C. A mixture of 0.55 part of pentaglycol diacid chloride and 10 parts of propionyl chloride was added dropwise to the suspension. 18 parts of propionyl chloride were then added and the mixture was heated at '7585 C. for 2 hours. The product, after being leached with water, occurred in the form of a white, fibrous mass (yield: about 99% based on tri-propionate) which was soluble in acetone; had a softening range of 155160 C., and which became rubberlike at 220-240 C.
  • Example IX The procedure was the same as described in Example VIII except that a mixture of 0.8 part of pentaglycol diacid chloride and 10 parts of propionyl chloride was added to the wood pulp suspension.
  • the final product (yield: 96% based on tripropionate) was a white, fibrous mass which formed a grainy solution in acetone, and had a softening range of -165 C.
  • Example X The reaction was carried out in the manner described in Example VIII with the exception that a mixture of 1.12 parts of hexaglycol diacid chloride and 10 parts of propionyl chloride was added to the wood pulp suspension.
  • the process comprising simultaneously reacting cellulose with at least one monobasic organic acid, and at least one polybasic organic acid in the presence of at least-one anhydride of a halogen-substituted monobasic organic acid, a
  • reaction 8 "product is at least partially solvated'during the reaction.
  • n is an integer
  • atleast one monobasic organic acid in the presence of at least one anhydride of a halogen-substituted monobasic organic acid, a catalyst, and a substance in which the reaction product is at least partially solvated during the reaction.
  • the process comprising simultaneously 'reacting cellulose with at least one monobasic 'organic acid, and at least one polybasic organic acid, in the presence of at least one anhydride of a halogen-substituted monobasic organic acid, a catalyst, and a substance in which the reaction product is at least partially solvated during the reaction, and terminating the reaction when substantially a monobasic acid triester has been formed and the polybasic organic acid radicals have combined with the cellulose in a ratio of about one such'radical per at least twenty anhydro-glucose unit's.

Description

formed under stress, and
Patented Dec. 27, 1949 UNITED STATES PATENT OFFICE PROCESS FOR THE PRODUCTION OF CELLULOSE ESTERS George A. Richter, Jr.,
to American Viscose Corporation,
Springfield, Pa., assignor Wilmington,
Del., a corporation of Delaware No Drawing. Original application March 16,
1944, Serial No. plication March 3 Claims.
from agents which are capable of reacting bifunctionally with cellulose.
Cellulose fibers have an extremely high degree of plasticity which is accompanied by low elasticity, and tend to undergo irreversible flow under moderate stresses. Products molded from cellulose or its derivatives, such as cellulose esters, exhibit the same properties and tend to become dethis tendency is not reversed and the products do not revert to their original form when the stress is removed.
I have now prepared a series of modified cellulose esters which also contain chemically bound radicals derived from agents which are capable of reacting bifunctionally with cellulose, the properties of which are radically different from those of cellulose or umnodified esters thereof, in that in the new products the high degree of plasticity which is a distinguishing characteristic of cellulose or cellulose esters is modified in favor of a greatly enhanced elasticity.
The esters preferably contain from about one or less than one radical derived from the agent capable of reacting bifunctionally with cellulose per about anhydro glucose units to one or less than one such radical per 500 anhydro glucose units or more. Of course, the ratio of the modifying radicals to glucose units may vary, but
where the ratio is substantially higher than one I in 20, the resulting product is extremely rigid and nonplastic.
In accordance with the invention, the radicals derived from agents capable of reacting bifunctionally with cellulose may be introduced simultaneously with or, in some cases, prior to the production of the esters.
According to one embodiment of the invention, at least one monobasic organic acid radical and at least one polybasic organic acid radical are introduced simultaneously into cellulose by reaction thereof with a monofunctional esterifying reagent and an esterifying agent capable of re- "acting bifunctionally with cellulose, the reaction being carried out in the presence of a substance in which the reaction product is at least partially solvated, that is, dissolved or swollen as it is formed during the reaction.
Suitable monofunctional reagents are monobasic organic acids, such as acetic, propionic,
526,812. Divided and this ap- 7, 1947, Serial No. 733,203
butyric, lauric acids, etc., anhydrides of such acids, and acid halides derived therefrom.
Suitable bifunctionally reacting agents are such polybasic organic acids as adipic, succinic, sebacic acids, etc., as well as polyhalides of such acids.
Diacids derived from glycol, as well as dihalides thereof, such as compounds having the general formula XOCCI-IzCI-Iz OCHzCHz) nCHZCHZCOX where X is hydroxyl or halogen and n is any integer but preferably from 1 to 4, inclusive, may also be used. Such diacids derived from glycol may be prepared by the general procedure described by Bruson, Journal American Chemical Society 64, pages 2457 and 2850.
In accordance with the invention, celluloseis simultaneously reacted with at least one polybasic organic acid, and at least one anhydride of a monobasic organic acid capable of esterifying cellulose, in the presence of a catalyst, which may be a mineral acid catalyst, for example, and a substance in which the reaction product is dissolved or swollen. during the reaction. Alternatively, the cellulose may be simultaneously reacted With at least one monobasic organic acid, and at least one polybasic organic acid, in the presence of an impeller which may be an anhydride of a halogen-substituted monobasic organic acid, a catalyst, and a substance in which the reaction product is dissolved or swollen during the reaction.
Acid halides may also be used. Thus, the cellulose may be reacted simultaneously with at least one monobasic organic .acid halide, and at least one polybasic organic acid halide, in the presence of a condensing agent which is inert with respect to the halides, such as an organic base as for instance, the tertiary amines, pyridine, quinoline, n-methyl morpholine, etc., in the presence of a solvent or swelling agent for the reaction product.
According to another embodiment of the in; vention, introduction of the polybasic organic acid radicals may be effected, in some cases, prior to esterification of the cellulose with a monobasic organic acid. Thus, cellulose may be reacted with one or more diacids derivedfromglycol, or dihalides of suchacids, in the presence of a condensing agent or catalyst, and the product thus obtained may then be subsequently reacted with at least one monobasic organic acid, in the usual manner.
An important feature of the invention is that the reaction is carried out in the presence of a substance in which the reaction product is dissolved or swollen as it is formed during the course of the reaction, which results inthe reaction mass being maintained ina highly swollen or dissolved state and thus insures substantially uniform reaction between the cellulose and the monofunctional and bifunctional reagents. Such substances are, for example, toluene, dioxane, acetone, etc. The final products which may be obtained by precipitating thereaction. mass from. water, may be soluble or substantially insoluble in such substances.
The amount of monofunctional reagent used may vary, but in general I prefer'to use an amount thereof sufiicient to form a tri-ester;
If a more lowly esterified final product is desired, such as a secondary or mono ester, the tri-ester may be suitably hydrolyzed by conventional methods, after'completion of. the reaction with the bifunctionally reacting esterification agent.
By the choice of bifunctional esterification agent; and the amount thereof participatin in thereaction, it is possible to selectively adjust certain physical properties of the final products, such as solubilities and softening temperatures. Althoughin-all cases the-modified esters show a lesser degree of plasticity and a greater degree of elasticity, and. in general much. higher softening and melting temperatures and resistance to common solvents, as compared with corresponding cellulose esters which do not contain the modifying-groups, modified esters may also be obtained which do not greatly differ from the unmodified l esters in respect of solubility and softening temperatures. The degree to whichthe final modified esters are soluble in substances which are solvents for cellulose esters, such as acetone, dioxane, toluene; etc., for instance, may vary, depending upon the amount of bifunctional esterification agent used, greater amounts decreasing the solubility and lesser amounts increasing it. Thus,
'final products may be obtained which form smooth relatively clear solutions in solvents such as acetone, toluene, dioxane, etc., or which form extremely viscous gel-like masses therein. Also, final products may be obtained which are insoluble in such common solvents or which are merely swollen slightly when added thereto. Generally speaking, the modified esters do not have melting points below decomposition temperatures or sharp softening points, are substantially unafiected at temperatures at which the unmodified esters melt or' soften, do not show a tendency to soften except within high temperature ranges, and at temperaturesabove the softening range are less plasticand more rubberlike than unmodified esters. However, the softening temperature in some instances may be varied, dependin upon. the amount and. type of bifunctional esterification agent used,.the tendency to soften at relatively low temperatures being more marked in those cases. wheresuch agent is used in relatively smallamounts and has a longer chain as compared to the ester side chain derived from the. monobasic acid. The use of marginal amounts of the bifunctional esterification agent in. the reaction thus permits a sensitive adjustment of the solubility and soft ening characteristics of the end, product. The amount of such agent to be used depends upon the properties desired in the final products. In
general to achieve the obiectives ofthis invention.
it is desirable to use the bifuncti'onally reacting agent, such as the dihalide of an organic dibasic acid, in amounts varying from 4 10- to about 4= lil mols thereof per 5 gms. of cellulose, the final product containing, usually, one or less than one dibasic acid radical. per 20 anhydro glucose units, to one or less than one dibasic acid radical per 500 anhydro glucose units, or more.
The products are obtained in the form of fibrous masses which are, for the most part, insoluble, infusible, and heat-insensitive, but which in certain cases, as previously indicated, may be soluble to varying extents and more or less susceptible to softening by heat.
Some of the insoluble or substantially insoluble modified esters, such as cellulose butyrate containin sebacic acid radicals may be molded by compression and injection molding techniques to give molded articles which are characterized by hardness, resistance to cold flow, and resistance to flow at elevated. temperatures. The molded products may undergosome flow under stress but due to their quality of rapid and-substantially complete elastic recovery, show a. lively return to their original form. upon the removal of. stress.
Those products which. are soluble. in-. solvents such as acetone, for example, may be dissolved therein and extruded through a-spinneret or the like into an evaporative atmosphere, in accordance with the dry-spinning process,.to form artificial filaments, or may be cast from such solutions to give films, sheets, coatings etc.. which are durable and stable.
If desired, substances may be added to the products to give various effects. Some of. the
' substances which may be added. are suitable coloring materials, such as dyes, pigments, particles of colored materials to give-mottled effects, metallic particlesorthe like.
The products exhibit properties suchas alesser degree of plasticity, greatly increased. elasticity, generally increased softening. and melting. temperature ranges, and rang of. solubilit incommon solvents which are. distinctly diflierent. from the properties of corresponding, cellulose. esters, such as cellulose laurate, cellulose propionate, etc., which do not containthe. chemically cornbined modifying polybasic acid radicals. While the reasons for the marked changein properties cannot be stated precisely, itisbelieved that the change may be predicated. upon. a chemica1.reaction of the polybasicacidsortheir halides-with hydroxyl groups on parallel. cellulosechains, so that cross-links are formedbetween the primary valence chains of. the. cellulose derivatives.
As previously indicated, the introduction'of the radical or radicals. derivedfrom thebifunctional esterification agent may be effected simultaneously with, or in some instances, prior to substantial esterification of the. cellulose. with the monobasic acids or their. halides, when the reaction is carried out.in.the presence ofasolveht capable of swelling, or dissolving the reaction product as: it is formed. during the reaction. However, it has not been. foundpracticable to efifect chemical.combinationofl the polybasic. acid radicals in the. case oi pre-shaped cellulose. esters, and the more highly esterified. the starting material he greater is the difiiculty encountered.
1t that the poly-functional esterification agents, suchas polyhalidesof polybasic acids, react chemically with. the free hydroxyls of previously shaped partiallyv esterified cellulose. only with considerable dificulty, iffati all, and that in all cases where shaped masses, fibers or the like consisting of or comprising partially esteriand leaching with water the reaction tri-laurate) was obtained fled cellulose have been treated with polybasic acids or their polyhalides in the absence of an agent which is capable of dissolving or swelling the reaction product as it is formed, only super- Example I Five parts of air-dry wood pulp were suspended in a mixture of 50 parts of pyridine and 100 parts of toluene and the suspension was heated to 70-80 C. A solution of 0.1 part of adipyl chloride in toluene was added to 40 parts of lauroyl chloride. The mixture was added dropwise to the above suspension, and the whole was heated to IS-85 C. for 4 hours. After precipitating and leaching with water, the reaction product (yield: 75% based on trilaurate) was obtained as a fibrous white mass which was substantially insoluble in toluene, did not soften below 140 C., and had no melting point. Unmodified cellulose laurate prepared under similar conditions softened at about 65 C.
Example II The reaction was carried out in accordance with the procedure described in Example 1, except that a 5% solution of 0.1 part of sebacoyl chloride were added to 40 parts of lauroyl chloride, and that mixture was added dropwise to the Wood pulp suspension. After precipitating product (yield: 87% based on as a fibrous white mass which was insoluble in toluene, did not soften below 210 0., and had no melting point.
Example III Eight parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and 100 parts of dioxane, and the suspension was heated to 60 to 80 C. A 5% solution of 0.06 part of sebacoyl chloride in toluene was added to 32 parts of butyryl chloride, and that mixture was added dropwise, with constant stirring, to the suspension. The mixture was heated to IS-85 C. for 2 hours. The reaction product (yield: 83% based on tri-butyrate) was precipitated and leached with water and a fibrous white mass was obtained, which was insoluble in acetone, and had a softening range of 130-135 C. The softening range of unmodified \cellulose butyrate prepared under similar conditions was found to be 125-l30 C.
Example IV The procedure was the same as described in Example III except that a 5% solution of 0.01 part of sebacoyl chloride was added to 32 parts of butyryl chloride, and that mixture was added drop-Wise to the wood pulp suspension. The final product (yield: about 91% based on tributyrate) was precipitated and leached with water. A fibrous white mass was obtained which was soluble in acetone, had a softening range of 130-135 C., and could be drawn into filaments at 180-200" C.
Example V Five parts air-dry wood pulp were suspended in a mixture of 50 parts of pyridine and 80 parts of dioxane and the suspension was heated to 60-85" C. A mixture of 26 parts of caproyl chloride and 0.08 part of succinyl chloride was addpionate) was a fibrous white mass ed dropwise to the above suspension, and the whole was heated at '75-85 C. for about 3 hours. After precipitating and leaching with water, the product was obtained as a white fibrous mass (yield: about 6% based on tricaproate). The product formed a very stiff gel in dioxane, and had a softening range of 120-l30 C. Unmodifled cellulose caproate prepared under similar conditions softened at about C.
Example VI Five parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and parts of dioxane, and the suspension was heated to 60-80 C. 0.2 part of hexaglycol diacid chloride was mixed with 28 parts of propionyl chloride, and added dropwise to the wood pulp suspension: the mixture was kept at 75-85" C. for 3 hours. After precipitating. and leaching with water the final product (yield:-97% based on tri-propionate) occurred in the form of a white mass which was soluble in acetone, had a softening range of -l60 C., and could be drawn to coarse filaments at about 200 C.
Example VII Five parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and 100 parts of dioxane, and the suspension was heated to 60-80 C. A mixture of 0.6 part of triglycol diacid chloride and 28 parts of propionyl chloride was added dropwise to the suspension, and the whole was heated at 75-85 C. for 2% hours. After precipitating and leaching the reaction product with water, a fibrous white mass was obtained (yield: 99% based on tri-propionate). The product formed a. grainy solution in acetone, and had softenin range of l55-160 C. Unmodified cellulose propionate softened at about 155 C.
Example VIII Five parts of air-dry wood pulp were suspended in a mixture of 80 parts of pyridine and 100 parts of dioxane, and the suspension was heated to 60-80 C. A mixture of 0.55 part of pentaglycol diacid chloride and 10 parts of propionyl chloride was added dropwise to the suspension. 18 parts of propionyl chloride were then added and the mixture was heated at '7585 C. for 2 hours. The product, after being leached with water, occurred in the form of a white, fibrous mass (yield: about 99% based on tri-propionate) which was soluble in acetone; had a softening range of 155160 C., and which became rubberlike at 220-240 C.
Example IX The procedure was the same as described in Example VIII except that a mixture of 0.8 part of pentaglycol diacid chloride and 10 parts of propionyl chloride was added to the wood pulp suspension.
The final product (yield: 96% based on tripropionate) was a white, fibrous mass which formed a grainy solution in acetone, and had a softening range of -165 C.
Example X The reaction was carried out in the manner described in Example VIII with the exception that a mixture of 1.12 parts of hexaglycol diacid chloride and 10 parts of propionyl chloride was added to the wood pulp suspension.
The product (yield: 76% based on tri-prowhich was solsolved in '50 parts of .glacial acetic acid for 2 hours at 3845=C. afterwhich '11.5-parts of glacial acetic acid and 0.02 part of sulfuric acid were added. The temperature was maintained at about Bil-45C. fr 1 /z hours, and then permitte'd to drop to 30 C., and maintained there 'for 1 4; hours. The mass was cooled to 18 0.
About 25.7parts of acetic acid anhydride cooled to 0- C.'w'ere added. The mass was then cooled 130 C., and a'mixture oi-0.33 part-of sulfuric acid and 0.57 part of glacial acetic acid was stirred int'o'the'inass, and the mixture was kept at C. for'about .i hours. -Averyfibrous white mass was thus obtained. A mixture of 7 parts "of sulfuric acid and 7 parts of glacial acetic acid was added, to hydrolyze the product to a secondary acetate. The hydrolyzed material was placed in a water bath at 40 C. for 24 7 hours. The mass was thinned with a little acetoneand precipitated by stirring in water; the
precipitate was washed and dried. The product did not have a"melting'point below decomposition; had a softenin range of about '230235 "0., and was insoluble inacetorie.
The above-examples and description are given by way-of illustration, and modifications or variations may be made therein without departing from the spirit and scope of the invention as defined in -the'claims.
I'claim:
'1. The process comprising simultaneously reacting cellulose with at least one monobasic organic acid, and at least one polybasic organic acid in the presence of at least-one anhydride of a halogen-substituted monobasic organic acid, a
- catalyst, and a substance in which the reaction 8 "product is at least partially solvated'during the reaction.
'2. The process comprising simultaneously reacting cellulose with 'atleast one poly'basic organic acid of the'general formula:
HOOCCHzCI-Iz (OCI-IzCHz) nOCI-I2CH2COOH where n is an integer, and atleast one monobasic organic acid, in the presence of at least one anhydride of a halogen-substituted monobasic organic acid, a catalyst, and a substance in which the reaction product is at least partially solvated during the reaction.
3. The process comprising simultaneously 'reacting cellulose with at least one monobasic 'organic acid, and at least one polybasic organic acid, in the presence of at least one anhydride of a halogen-substituted monobasic organic acid, a catalyst, and a substance in which the reaction product is at least partially solvated during the reaction, and terminating the reaction when substantially a monobasic acid triester has been formed and the polybasic organic acid radicals have combined with the cellulose in a ratio of about one such'radical per at least twenty anhydro-glucose unit's.
GEORGE A. RICHTER, JR.
REFERENCES CITED The following "references are of record in "the file of this patent:
UNITED STATES PATENTS Number Name Date 1,950,664: Dreyfus'et'al Mar. '13, 1934 2,000,621 Staudet a1 May 7, 1935 FOREIGN PATENTS Number Country Date 531674 -Great Britain u Jan. .29, 1941 Certificate of Correction Patent N 0. 2,492,443 December 27, 1949 GEORGE A. RICHTER, JR.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows:
Column 6, line 5, for 6% read 66%;
and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 4th day of July, A. D. 1950.
THOMAS F. MURPHY,
Assistant Gammissioner 0/ Patents.
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1950664A (en) * 1929-08-27 1934-03-13 Celanese Corp Treatment of textile and other material
US2000621A (en) * 1933-01-14 1935-05-07 Eastman Kodak Co Propionation of cellulosic material
GB532674A (en) * 1939-07-18 1941-01-29 Henry Dreyfus Improvements in or relating to the production of acidyl derivatives of cellulose andother organic substances

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1950664A (en) * 1929-08-27 1934-03-13 Celanese Corp Treatment of textile and other material
US2000621A (en) * 1933-01-14 1935-05-07 Eastman Kodak Co Propionation of cellulosic material
GB532674A (en) * 1939-07-18 1941-01-29 Henry Dreyfus Improvements in or relating to the production of acidyl derivatives of cellulose andother organic substances

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